ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.302-13C>T

gnomAD frequency: 0.68152  dbSNP: rs3735953
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000254101 SCV000311830 benign not specified criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000254101 SCV000540694 benign not specified 2016-03-29 criteria provided, single submitter clinical testing Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency
GeneDx RCV001668526 SCV001885834 benign not provided 2018-11-13 criteria provided, single submitter clinical testing
Invitae RCV002058228 SCV002484962 benign 46,XY sex reversal 9 2024-02-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002058228 SCV002514100 benign 46,XY sex reversal 9 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002244630 SCV002514101 benign Tetralogy of Fallot 2021-12-05 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000254101 SCV003928347 benign not specified 2023-04-04 criteria provided, single submitter clinical testing

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